Canonical Allele Identifier: CA2437510028

Gene: SLC16A2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74531334C= , CM000685.2:g.74531334C=	GRCh38
NC_000023.10:g.73751169C= , CM000685.1:g.73751169C=	GRCh37
NC_000023.9:g.73667894C=	NCBI36
NG_011641.1:g.115085C=
NG_011641.2:g.115085C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000587091.6:c.1401C= MANE Select	ENSP00000465734.1:p.Gly467=
ENST00000636771.1:c.1310C=
ENST00000587091.5:c.1401C=	ENSP00000465734.1:p.Gly467=
ENST00000590447.1:c.612C=
NM_006517.4:c.1401C=	NP_006508.2:p.Gly467=
XM_005262294.1:c.1172C=	XP_005262351.1:p.Ala391=
NM_006517.5:c.1401C= MANE Select	NP_006508.2:p.Gly467=